A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25786417



Internal ID18826942
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:10528083..10640166hg38UCSC Ensembl
Innerchr16:10621940..10734023hg19UCSC Ensembl
Innerchr16:10529441..10641524hg18UCSC Ensembl
Cytoband16p13.13
Allele length
AssemblyAllele length
hg38112084
hg19112084
hg18112084
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3892791
Supporting Variants
Samples
Known GenesEMP2, TEKT5
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=56
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25786417
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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